Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:2374891rdf:typepubmed:Citationlld:pubmed
pubmed-article:2374891lifeskim:mentionsumls-concept:C0002726lld:lifeskim
pubmed-article:2374891lifeskim:mentionsumls-concept:C0086981lld:lifeskim
pubmed-article:2374891pubmed:issue27-28lld:pubmed
pubmed-article:2374891pubmed:dateCreated1990-8-24lld:pubmed
pubmed-article:2374891pubmed:abstractTextWe report on two patients with rheumatoid arthritis and sicca syndrome due to secondary amyloidosis (A-amyloid) with involvement of the kidneys and gut. At autopsy, generalized amyloidosis was found with deposits in the salivary and lacrimal glands. Two other patients developed sicca syndrome due to primary systemic L-amyloidosis with Bence-Jones paraproteinuria, renal insufficiency and amyloid cardiomyopathy; both died of cardiac failure. Although sicca syndrome with amyloidosis has been described only occasionally, it is possible that this association is more frequent. These observations suggest that not only Sjögren's syndrome but also amyloidosis should be considered as a possible cause of sicca syndrome.lld:pubmed
pubmed-article:2374891pubmed:languagegerlld:pubmed
pubmed-article:2374891pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2374891pubmed:citationSubsetIMlld:pubmed
pubmed-article:2374891pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2374891pubmed:statusMEDLINElld:pubmed
pubmed-article:2374891pubmed:monthJullld:pubmed
pubmed-article:2374891pubmed:issn0036-7672lld:pubmed
pubmed-article:2374891pubmed:authorpubmed-author:GebbersJ OJOlld:pubmed
pubmed-article:2374891pubmed:authorpubmed-author:MaroniGGlld:pubmed
pubmed-article:2374891pubmed:authorpubmed-author:RamelliG PGPlld:pubmed
pubmed-article:2374891pubmed:issnTypePrintlld:pubmed
pubmed-article:2374891pubmed:day10lld:pubmed
pubmed-article:2374891pubmed:volume120lld:pubmed
pubmed-article:2374891pubmed:ownerNLMlld:pubmed
pubmed-article:2374891pubmed:authorsCompleteYlld:pubmed
pubmed-article:2374891pubmed:pagination995-8lld:pubmed
pubmed-article:2374891pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:2374891pubmed:meshHeadingpubmed-meshheading:2374891-...lld:pubmed
pubmed-article:2374891pubmed:meshHeadingpubmed-meshheading:2374891-...lld:pubmed
pubmed-article:2374891pubmed:meshHeadingpubmed-meshheading:2374891-...lld:pubmed
pubmed-article:2374891pubmed:meshHeadingpubmed-meshheading:2374891-...lld:pubmed
pubmed-article:2374891pubmed:meshHeadingpubmed-meshheading:2374891-...lld:pubmed
pubmed-article:2374891pubmed:meshHeadingpubmed-meshheading:2374891-...lld:pubmed
pubmed-article:2374891pubmed:meshHeadingpubmed-meshheading:2374891-...lld:pubmed
pubmed-article:2374891pubmed:meshHeadingpubmed-meshheading:2374891-...lld:pubmed
pubmed-article:2374891pubmed:meshHeadingpubmed-meshheading:2374891-...lld:pubmed
pubmed-article:2374891pubmed:year1990lld:pubmed
pubmed-article:2374891pubmed:articleTitle[Sicca syndrome in amyloidosis].lld:pubmed
pubmed-article:2374891pubmed:affiliationMedizinische Klinik, Kantonsspital Luzern.lld:pubmed
pubmed-article:2374891pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2374891pubmed:publicationTypeEnglish Abstractlld:pubmed
pubmed-article:2374891pubmed:publicationTypeCase Reportslld:pubmed